NUDT17

NUDT17
Identifiers
Aliases	NUDT17 , nudix hydrolase 17
External IDs	MGI: 1925623 HomoloGene: 45961 GeneCards: NUDT17
Gene location (Human)
Chr.	Chromosome 1 (human)
End	145,848,954 bp
Gene location (Mouse)
Chr.	Chromosome 3 (mouse)
End	96,615,878 bp
RNA expression pattern
	Top expressed in
	vagina; ; ovary; ; testicle; ; prosencephalon; ; muscle tissue; ; cerebellar hemisphere; ; cerebellum; ; tendon;
	More reference expression data
	n/a
Gene ontology
Molecular function	hydrolase activity ; metal ion binding ; NADH pyrophosphatase activity ;
Cellular component	peroxisome ; cytosol ;
Biological process	NADH metabolic process ; NADP catabolic process ; NAD catabolic process ;
	Sources:Amigo / QuickGO
Orthologs
	200035
	78373
	ENSG00000186364
	ENSMUSG00000028100
	P0C025
	Q9CWD3
	NM_001012758
	NM_001162925 ; NM_030094
	NP_001012776
	NP_001156397 ; NP_084370
	Wikidata
View/Edit Human	View/Edit Mouse

Last updated April 09, 2022

Nudix hydrolase 17 is a protein that in humans is encoded by the NUDT17 gene. ^[5]

Related Research Articles

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Bis(5'-nucleosyl)-tetraphosphatase [asymmetrical] is an enzyme that in humans is encoded by the NUDT2 gene.

Diphosphoinositol polyphosphate phosphohydrolase 3-beta is an enzyme that in humans is encoded by the NUDT11 gene.

Homeobox protein Hox-C11 is a protein that in humans is encoded by the HOXC11 gene.

ADP-ribose pyrophosphatase, mitochondrial is an enzyme that in humans is encoded by the NUDT9 gene.

Diphosphoinositol polyphosphate phosphohydrolase 2 is an enzyme that in humans is encoded by the NUDT4 gene.

Diphosphoinositol polyphosphate phosphohydrolase 1 is an enzyme that in humans is encoded by the NUDT3 gene.

ADP-sugar pyrophosphatase is an enzyme that in humans is encoded by the NUDT5 gene.

Mitochondrial glycine transporter is a protein that in humans is encoded by the SLC25A38 gene. SLC25A38 is involved in mitochondrial handling of glycine and is needed for the first step in heme synthesis. Mutations in this gene can lead to an autosomal recessive form of sideroblastic anemia.

Zinc finger and BTB domain containing 11 is a protein that in humans is encoded by the ZBTB11 gene.

BarH-like homeobox 2 is a protein in humans that is encoded by the BARHL2 gene.

Inositol monophosphatase 3 also known as inositol monophosphatase domain-containing protein 1 (IMPAD1) is an enzyme that in humans is encoded by the IMPAD1 gene.

GNPTG is a gene in the human body. It is one of three genes that were found to correlate with stuttering.

Solute carrier family 15, member 4 is a protein in humans that is encoded by the SLC15A4 gene.

GDNF family receptor alpha-4 (GFRα4), also known as the persephin receptor, is a protein that in humans is encoded by the GFRA4 gene.

Forkhead box B1 is a protein that in humans is encoded by the FOXB1 gene.

Ubiquitin specific peptidase 19 is a protein that in humans is encoded by the USP19 gene.

Forkhead box Q1 is a protein that in humans is encoded by the FOXQ1 gene.

Haloacid dehalogenase like hydrolase domain containing 5 is a protein that in humans is encoded by the HDHD5 gene.

Forkhead box S1 is a protein that in humans is encoded by the FOXS1 gene.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000186364 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000028100 - Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Entrez Gene: Nudix hydrolase 17" . Retrieved 2017-06-30.

NUDT17

Related Research Articles

References

Further reading